Canonical Allele Identifier: CA2617597924

Gene: CLEC12B

Linked Data

• gnomAD v4: 12-10018079-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10018081del , CM000674.2:g.10018081del	GRCh38
NC_000012.11:g.10170680del , CM000674.1:g.10170680del	GRCh37
NC_000012.10:g.10061947del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-250del MANE Select	ENSP00000344563.5:n.681-250del
ENST00000338896.10:c.681-250del	ENSP00000344563.5:n.681-250del
ENST00000338896.9:c.681-250del	ENSP00000344563.5:n.681-250del
ENST00000544853.5:c.*129-250del	ENSP00000439561.1:n.*129-250del
NM_001129998.1:c.681-250del	NP_001123470.1:n.681-250del
NR_120484.1:n.249-2307del
XM_006719070.2:c.681-337del	XP_006719133.1:n.681-337del
XM_006719071.2:c.*3-250del	XP_006719134.1:n.*3-250del
XM_011520658.1:c.654-250del	XP_011518960.1:n.654-250del
XM_011520661.1:c.*10-250del	XP_011518963.1:n.*10-250del
XM_011520663.1:c.526-250del	XP_011518965.1:n.526-250del
XM_011520664.1:c.526-337del	XP_011518966.1:n.526-337del
XR_242889.3:n.956-250del
NM_001129998.2:c.681-250del	NP_001123470.1:n.681-250del
NM_001319241.1:c.372-250del	NP_001306170.1:n.372-250del
NR_135049.1:n.961-250del
XM_011520658.2:c.654-250del	XP_011518960.1:n.654-250del
XM_011520663.2:c.526-250del	XP_011518965.1:n.526-250del
XM_017019295.1:c.372-250del	XP_016874784.1:n.372-250del
XM_024448976.1:c.681-337del	XP_024304744.1:n.681-337del
XR_002957401.1:n.106-1932del
NM_001129998.3:c.681-250del MANE Select	NP_001123470.1:n.681-250del
NM_001387138.1:c.681-337del	NP_001374067.1:n.681-337del
NR_169587.1:n.258-1932del